Averantin
Product Code:
BVT-0169
BVT-0169
Regulatory Status:
RUO
RUO
Shipping:
Ambient
Ambient
Storage:
+4°C
+4°C
No additional charges, what you see is what you pay! *
| Code | Size | Price |
|---|
| BVT-0169-M001 | 1 mg | £95.00 |
Quantity:
| BVT-0169-M005 | 5 mg | £350.00 |
Quantity:
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This product comes from: Switzerland.
Typical lead time: 10-14 working days.
Contact us for more accurate information.
Typical lead time: 10-14 working days.
Contact us for more accurate information.
- Further Information
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Further Information
Alternate Names/Synonyms:
BRN 2309929; 2-(1-Hydroxyhexyl)-1,3,6,8-tetrahydroxyanthraquinone
Appearance:
Orange powder.
CAS:
5803-62-3
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Protect from light.
Hazards:
H302, H312, H319
InChi:
InChI=1S/C20H20O7/c1-2-3-4-5-12(22)17-14(24)8-11-16(20(17)27)19(26)15-10(18(11)25)6-9(21)7-13(15)23/h6-8,12,21-24,27H,2-5H2,1H3/t12-/m0/s1
InChiKey:
WGPOPPKSQRZUTP-LBPRGKRZSA-N
Long Description:
Chemical. CAS: 5803-62-3. Formula: C20H20O7. MW: 372.4. Isolated from Aspergillus sp. (strain WDMH51). Mycotoxin. Intermediate of the biosynthetic pathway to aflatoxin B1. Cytotoxic against human solid tumor cell lines.
MDL:
MFCD01664488
Molecular Formula:
C20H20O7
Molecular Weight:
372.4
Package Type:
Plastic Vial
Precautions:
P270, P280, P301, P312, P302, P352, P312
Product Description:
Mycotoxin. Intermediate of the biosynthetic pathway to aflatoxin B1. Cytotoxic against human solid tumor cell lines. Moderate antifungal and antibacterial agent.
Purity:
>98% (HPLC; NMR)
Signal word:
Warning
SMILES:
CCCCC[C@H](O)C1=C(O)C2=C(C=C1O)C(=O)C1=C(C(O)=CC(O)=C1)C2=O
Solubility Chemicals:
Soluble in acetone, methanol or DMSO.
Source / Host:
Isolated from Aspergillus sp. (strain WDMH51).
Transportation:
Non-hazardous
UNSPSC Category:
Natural Products/Extracts
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C.
Documents
References
Product B (Averantin), a pigment from Aspergillus versicolor: J.H. Birkinshaw, et al.; J. Chem. Soc. (C) 1966, 855 (1966) | Stereochemical correlation of (-)-averantin: C.A. Townsend & S.B. Christensen; Tetrahedron Lett. 27, 887 (1986) | A reappraisal of fungi producing aflatoxins: J. Varga: World Mycotoxin J. 2, 263 (2009) | Bioactive metabolites from the sponge-derived fungus Aspergillus versicolor: Y.M. Lee, et. al; Arch. Pharm. Res. 33, 231 (2010) | Genetics of polyketide metabolism in Aspergillus nidulans: M.L. Klejnstrup, et al.; Metabolites 2, 100 (2012) | The antifungal metabolites obtained from the rhizospheric Aspergillus sp. YIM PH30001 against pathogenic fungi of Panax notoginseng: K. Liu, et al.; Nat. Prod. Res. 28, 2334 (2014)
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